Genotoxicity and Histopathological Studies on the Liver and Kidney of Male Rats Fed on Diet Containing Waste Fat Released from Chicken During Grilling Process

Authors

  • G. M. HASSAN Genetics Dept., Fac. Agric., Fayoum Univ., Egypt
  • KH. M. MAZHER Cytol. Histol. Dept., Fac.Vet. Med., Beni Suif Univ., Egypt

Abstract

Food is essential to provide sustenance but may also be an important
factor in the genesis of human diseases. An association between the intake of grilled or broiled meat and development of cancer was recorded by Thomson et al. (1996).
Grilling meat, fish or other foods with intense heat over a direct flame result in fat dripping on the hot fire and yielding flames containing a number of polycyclic hydrocarbons (PAHs), these chemicals adhere to the surface of the food. The more intense the heat, the more PAHs are present (Larsson, 1986). PAHs are produced from organic compounds by condensation of smaller units at high temperatures forming stable polynuclear aromatic compounds. At high temperature, organic compounds are easily fragmented into smaller compounds, mostly free radicals, which may then recombine to form a number of relatively stable PAHs (Lijinsky, 1991). Lin et al. (1996) showed that, mice fed high fat diet developed more serve disease and had a shorter life span.
Weisburger et al. (1994) found that the use of grilled meats in diet, where compounds formed on the surface of meat may be associated with increased risk of genotoxicity and cancer. They also showed that, normal intestinal bacteria can convert one of these compounds, 2-amino-3-methyl-3H-imidazo [4, 5-f] quinoline (IQ) to the 7-hydroxy metabolite, 2-amino-3,6-dihydro-3-methyl-7H-imida-zolo[4, 5-f] quinolin-7-one(7-OHIQ),a directacting mutagen.
The surface of fried and grilled meat or fish contain powerful mutagens, Sugimura et al. (1977) isolated these mutagens and identified them as heterocyclic aromatic compounds with an exocyclic amino group and often an O-methyl group.
The heterocyclic amines formed by partial pyrolysis of amino acids, sugar or creatinine at high temperatures has been shown to be carcinogenic and mutagenic in mice and rats (Ohgaki et al., 1991).
Food mutagens cause different types of DNA damage, nucleotide alterations and gross chromosomal aberrations. Most mutagens begin their action at the DNA level by forming carcinogen-DNA adducts, which result from the covalent binding of a carcinogen or part of a carcinogen to a nucleotide. However, the effect of food mutagens in carcinogenesis can be modified by heritable traits, namely, low penetrant genes that affect mutagen exposure of DNA through metabolic activation and detoxification or cellular responses to DNA damage through DNA repair mechanisms or cell death (Goldman and Shields, 2003)
The single cell gel electrophoresis (SCGE) assay, also known as the comet assay, is a rapid, simple, visual and sensitive technique for detecting and analyzing DNA strand breakage in a variety of organs and various mammalian cells (Olive et al., 1990). The advantage of the comet assay is that it allows any viable eukaryote cells to be analyzed. For these reasons, the comet assay is now widely used in researches of biomonitoring and DNA damage processes to routine assessments of genotoxicity. Quantitative analysis for DNA damage has yielded several parameters, including tailed nuclei, tail length, DNA % in the tail, and tail moment in the comet assay (Tice et al., 2000).
Singh et al. (1988) made microgels slides and electrophoresing under alkaline conditions and removed the DNA supercoiling and denaturated the DS DNA to SS DNA .With this modification they obtained a dose response curve with respect to length of DNA migration. The resulting images were subsequently named ‘Comet ‘because of their appearance and their total length was considered directly related to the DNA damage. From that moment a range of applications of the Comet assay have been used in investigations of the physiochemical behavior of DNA, through studies of cellular responses of DNA damage, to biomonitoring of human population.
When the Comet assay technique is used to detect in vivo genotoxicity, the most important advantage is that DNA lesions can be measured in cells not engaged in mitotic activity, making it possible to assay many organs (Fairbairn et al.,
1995).
The grilled chicken fat was used by low income people in Egypt and used to prepare Howawshi. Thus the aim of this study was to evaluate the genotoxic and histopathologic effects on liver and kidney of rats fed on diet contained fats of grilled chicken.

References

Aly, K. A. (1997). Physiological and histopathological effects of some synthetic food colouring additives in rats. PhD. Thesis, Faculty of Science, Cairo University.

AOAC, (1990). Official method of analysis (15th ed.). Association of official analytical chemisits, Virginia,

DC.

Attia, Z. I., M. A. Basyuni, M. A. Hegazi and S. G. Okba (2005). Effects of benzene sulfonic acid the physiology and growth rate of young rats. Egypt. J. Zool., 45: 373-387.

Bancroft, J. D. and M. Gamble (2002). Theory and practice of histological techniques. In: B. Swisher, Editor, Microorganisms, Churchill. Livingstone, Philadelphia, 325-344.

Brulles, S. and P. W. Wells (1977). In vitro stimulation of avian lymphocytes by various mitogens. Res. Vet. Sci., 23: 84-86.

Duncan, D. B. (1955). Multiple range and Multiple F tests. Biometrics, 11: 1-42.

Early, I. I., V. K. Novainakere and A. Weaver (1992). Effect of cadmium on liver mitochondria and rough endoplasmic reticulum in the rat. Toxicol. Lett., 62: 73-83

El-Shamy, K. A., M. E. Khadr, F. A. Morsy and M. M. Hassanin (1999). Toxic effects of some food additives of albino rat, green colours. Egypt. J. Zool., 32: 417-440.

Fairbairn, D. W., O. L. Peggy and K. L. Oneil (1995). The comet assay: a comprehensive review. Mutat. Res., 339: 37-39.

Feulgen, R. and H. Rossenbeck. (1924). Mikroskopisch nach weis einen nucleinsaure von typus thymonucleinsaure und de darauf berhende elective farbug von zelkernen in microskopischen preparaten. Zeitschrift Physiology Chemistry, 135: 203.

Ford, S. M., J. B. Hook and J. T. Bond (1980). The effect of butylated hydroxyanisole and butylated hydroxytoluene on renafunction in the rat. Food Cosmet. Toxicol., 18: 15-23.

Goldman, R. and P. G Shields. (2003). Food mutagens. J. Nutr. 133: 965-973.

Guidarelli, A., F. Cattabeni and O. Cantoni (1997). Alternative mechanism for hydroperoxide-induced DNA single strand breakage. Free Radic. Res. J., 26: 537-547

Hussein, T. D., M. A. Amer, A. S. Hamza and I. Samir (2007). Effect of erythrosine on the liver of albino mice. Egypt. J. Zool., 49: 1-21.

Klastskin, G. and H. Oconn. (1993). Abnormalities of the hepatic parenchyma. In Histopathology of liver . Vol. 1. Oxford Uni. Press, New York, p. 40-55.

Kaboglu, A. and T. Aktac (2002). A study of the effects of sodium benzoate on the mouse liver. Biologia Bratislava, 57: 373-380.

Larsson, B. K. (1986). Polycyclic aromatic hydrocarbons in Swedish foods. Aspects on analysis, occurrence and intake. Ph.D. thesis, Swedish University Sciences.

Lijinsky, W. (1991). The formation and occurrence of polynuclear aromatic hydrocarbons associated with food, Mutat. Res., 259: 251-

Lin, B. F., C. C. Huang, B. L. Chiang and S. J. Jeng (1996). Dietary fat influences Ia antigen expression, cytokine and prostaglandin E2 production of immune cells in autoimmune-prone NZB x NZW f1 mice. Brit. J. Nutr., 75: 711-722.

Mazia, D., P. A. Brewer and M. Alfert (1953). The cytochemical staining and measurement of protein with bromophenol blue. Bil. Bull., 104:

-67.

Ohgaki, H., S. Takayama and T. Sugimuro (1991). Carcinogenicities of heterocyclic amines in cooked food. Mutation Research, 259:

-410.

Olive, P. L., J. P. Banath and R. E. Durand (1990). Detection of etoposide resistance by measuring DNA damage in individual Chinese hamster cells. J. Nat. Cancer Inst., 82: 779-783.

Oslen, P., O. Meyer, N. Bille and G. Wurtyen (1986). Carcinogenicity study on BHT in Wister rat exposed in utero. Food Cosmet. Toxicol., 24: 1-18.

Rawat, D. K., M. F. Valim and N. C. Agrawal (2002). A correlative study on liver glycogen and endosulfan sulfan toxicity in Heteropes fossilis. J. Environ. Biol., 23: 5-11.

Sasaki, Y. F., S. Tsuda, F. Izumiyama and E. Nishidate (1997). Detection of chemically induced DNA lesions in multiple mouse organs using the alkaline single cell gel electrophoresis (Comet assay). Mutation research., 388: 33-44.

Sasaki, Y. F., S. Kawaguchi, A. Kamaya, M. Ohshita, K. Kabasawa, K. Iwama, K. Taniguchi and S. Tsuda (2002). The comet assay with 8 mouse organs: results with 39 currently used food additives. Muta. Res. Genetic Toxicol. Environ. Muta., 519: 103-119.

Selim, M. E. (2005). Monosodium glutamate-induced nephrotoxicity on young mice and the possible counteracting effect of barley. Egypt. J. Zool., 45: 101-121.

Sharma, S. D. and M. Iqbal. (2005). Lithium induced toxicity in rats. A hematological, biochemical and histopathological study. Biol. Pharm. Pathol., 28: 834-837.

Sharma, S. D., R. Goyal, G. Chakravarty and A. Sharma (2008). Toxicity of tomato red a popular food dye blend on male albino mice. Exp.Toxicol. Pathol., 60: 51-57.

Singh, N. P., M. T. MyCoy, R. R. Tice and E. L. Schneider (1988). A simple technique for quantification of low levels of DNA damage in

individual cells. Exp. Cell Res., 175: 184-191.

Sugimura, T., M. Nagao, T. Kawachi, M. Honda, T. Yahagi, Y. Seino, S. Sano, N. Matsukura, T. Matsushima, A. Usui, M. Sawamura and H. Matsumoto (1977). Mutagen-carcinogens in foods, with special reference to highly mutagenic pyrolytic products in broiled foods. In Hiatt, H. H., Watson, J.D. and Winsten, J. A. (Eds) Origins of Human Cancer. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, NY, p. 1561-1577.

Surzycki, S. (2000). In. Basic techniques in molecular biology preparation of genomic DNA from animal cells. Springer-verlag publications, Berlin-Heidelborg., 40-44.

SPSS (1999). Statistical software package for the social science SPSS, Inc., USA.

Thomson, B. M., R. J. Lake, P. J. Cressey and M. G. Knize (1996). Estimated cancer risk from heterocyclic amines in cooked meat a New Zealand perspective. Proceedings of the Nutrition Society, 21.

Tice, R. R., E. Agurell, D. Anderson, B. Burlinson, A. Hartmann, H. Kobayashi, Y. Miyamae, E. Rojas, J. C. Ryu and Y. F. Sasaki (2000). Single cell gel/Comet Assay: guidelines for in vitro and in vivo genetic toxicology testing. Environ. Mol. Mutagen, 35: 206-221.

Tsuda, S., M. Murakami, N. Matsusaka, K. Kano, K. Taniguchi and Y. Sasaki (2001). DNA damage induced by red food dyes orally administered to pregnant and male mice. Toxicol. Sci., 61: 92-99.

Villarini, M., M. Moretti and R. Pasquini (1998). In vitro genotoxic effects of the insecticide deltamethrin in human peripheral blood leucocytes: DNA damage (comet assay) in relation to the induction of sister chromatid exchanges and micronuclei. Toxicology, 130: 129-139.

Weisburger, J. H., A. Rivenson, J. Reinhardt, C. Aliaga, J. Braley, L. M. Dolan, G. M. Williams, E. Zong, and D. G. Kingston (1994). Genotoxicity and carcinogenicity in rats and mice of 2-amino-3, 6-dihydro-3-methyl-7H-imidazolo

, 5-f] quinoline-7-one: an intestinal bacterial metabolite of 2-amino-3-methyl-3H-imidazol [4, 5-f] quinolin. J. Natl. Cancer Inst.,

: 25-30.

Downloads

Published

2016-01-11

Issue

Section

Articles